Oromandibular dystonia

Symptom Information:

Symptom ID: HPO:0012048
Synonyms:
Cranial dystonia [HPO:0012048]
Cranial dystonia [OMIM:Cranial dystonia]
Oromandibular dystonia [OMIM:Oromandibular dystonia]
Oromandibular dystonia (in some patients) [OMIM:Oromandibular dystonia (in some patients)]
Oromandibular dystonia [MedDRA:10067954]
Quality:
Cross references:
OMIM: "Cranial dystonia" [OMIM:Cranial dystonia]
OMIM: "Oromandibular dystonia" [OMIM:Oromandibular dystonia]
OMIM: "Oromandibular dystonia (in some patients)" [OMIM:Oromandibular dystonia (in some patients)]
Is a (Direct Parents):
HPO         Craniofacial dystonia
MedDRA Dystonias
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of movement(HPO:0100022)
                Dystonia(HPO:0001332)
                   Focal dystonia(HPO:0004373)
                      Craniofacial dystonia(HPO:0012179)
                         Oromandibular dystonia(HPO:0012048)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Dystonias(MedDRA:10013985)
          Oromandibular dystonia(HPO:0012048)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant cervical dystonia (Orphanet:93962)
Autosomal dominant focal dystonia, DYT7 type (Orphanet:93963)
DYSTONIA 24 (OMIM:615034)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6 (OMIM:615643)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
Primary dystonia, DYT13 type (Orphanet:98807)
Primary dystonia, DYT6 type (Orphanet:98806)